CN103877964B - A kind of preparation method of the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and anatase phase titanium dioxide - Google Patents
A kind of preparation method of the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and anatase phase titanium dioxide Download PDFInfo
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- CN103877964B CN103877964B CN201410088477.XA CN201410088477A CN103877964B CN 103877964 B CN103877964 B CN 103877964B CN 201410088477 A CN201410088477 A CN 201410088477A CN 103877964 B CN103877964 B CN 103877964B
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 title claims abstract description 99
- NKZSPGSOXYXWQA-UHFFFAOYSA-N dioxido(oxo)titanium;lead(2+) Chemical compound [Pb+2].[O-][Ti]([O-])=O NKZSPGSOXYXWQA-UHFFFAOYSA-N 0.000 title claims abstract description 43
- 239000004408 titanium dioxide Substances 0.000 title claims abstract description 38
- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 49
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000002131 composite material Substances 0.000 claims abstract description 14
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000008367 deionised water Substances 0.000 claims abstract description 8
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 8
- 238000003756 stirring Methods 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 239000000725 suspension Substances 0.000 claims description 12
- 230000033228 biological regulation Effects 0.000 claims description 9
- 238000005406 washing Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 claims 1
- 239000010959 steel Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 9
- 230000003197 catalytic effect Effects 0.000 abstract description 4
- 230000007062 hydrolysis Effects 0.000 abstract description 4
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 4
- 238000001027 hydrothermal synthesis Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 3
- 238000010335 hydrothermal treatment Methods 0.000 abstract description 2
- 238000011031 large-scale manufacturing process Methods 0.000 abstract 1
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 5
- 229960000907 methylthioninium chloride Drugs 0.000 description 5
- 230000010287 polarization Effects 0.000 description 3
- 230000002269 spontaneous effect Effects 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000005286 illumination Methods 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 238000003421 catalytic decomposition reaction Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 239000002957 persistent organic pollutant Substances 0.000 description 1
- 238000007146 photocatalysis Methods 0.000 description 1
- 230000001699 photocatalysis Effects 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
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Abstract
The present invention relates to the preparation method of a kind of Perovskite Phase lead titanate monocrystal nano line and the hetero-junctions of anatase phase titanium dioxide, using the ethanol solution of tetra-n-butyl titanate and front Perovskite Phase lead titanate monocrystal nano line as the material of hydro-thermal reaction, anatase phase titanium dioxide is obtained by the hydrolysis of tetra-n-butyl titanate, using ammonia as mineralizer, and add the hydrolysis of deionized water promotion tetra-n-butyl titanate, it is then transferred in reactor carry out hydrothermal treatment consists, obtain the hetero-junctions of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide, again through follow-up high-temperature process, obtain the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide.Preparation process of the present invention is simple, it is easy to control, pollution-free, low cost, it is easy to large-scale production；In the composite prepared, titanium dioxide can preferably be grown on Perovskite Phase lead titanate monocrystal nano line, is evenly distributed；And visible light catalytic efficiency is higher.
Description
Technical field
The present invention relates to the preparation method of a kind of Perovskite Phase lead titanate monocrystal nano line and the hetero-junctions of anatase phase titanium dioxide, belong to field of inorganic nonmetallic material.
Background technology
Titanium dioxide is research and most widely used a kind of semiconductor light-catalyst, can be with catalytic decomposition water hydrogen manufacturing and degradable organic pollutant under illumination condition, but owing to its energy gap (energy gap of anatase phase titanium dioxide is 3.2eV) is relatively big, therefore ultraviolet light photons can only be absorbed.But, ultraviolet light only accounts for the 3% ~ 5% of sunlight, and visible ray accounts for the 43% of solar energy, therefore, as by TiO2The regulation of light degradation absorption bands will have important practical significance to visible light wave range.The energy gap of Perovskite Phase lead titanate monocrystal nano line is about 2.8eV, and it is in visible region, when TiO2When being combined into a kind of hetero-junctions with Perovskite Phase lead titanate monocrystal nano line, it is possible to utilizing lead titanates to produce electron hole pair to absorb light photon, electron hole pair moves to TiO again2Reaction is participated on surface, finally realizes TiO2Visible light catalytic.And Perovskite Phase lead titanates is one of material that in the ferroelectric being currently known, spontaneous polarization strength is the highest, the spontaneous polarization value actually observed during its room temperature reaches 75 μ C/cm2, and the spontaneous polarization in lead titanates ferroelectric domain enables to its band curvature, so that the electronics of illumination generation and hole migrate in the opposite direction, reduces electronics and the recombination probability in hole, thus finally improve the visible light catalytic efficiency of this kind of hetero-junctions.
Summary of the invention
It is an object of the invention to provide a kind of technique simple, process is easily controllable, it is seen that the preparation method of the higher Perovskite Phase lead titanate monocrystal nano line of photocatalysis efficiency and the hetero-junctions of anatase phase titanium dioxide.
The Perovskite Phase lead titanate monocrystal nano line of the present invention and the preparation method of the hetero-junctions of anatase phase titanium dioxide, comprise the following steps:
1) tetra-n-butyl titanate is dissolved in ethanol, regulate Ti4+Concentration is 0.035 ~ 0.082mol/L, and stirs to being completely dissolved；
2) Perovskite Phase lead titanate monocrystal nano line before adding in the ethanol solution of the tetra-n-butyl titanate prepared to step 1), regulation tetra-n-butyl titanate is 0.267 ~ 0.623:1 with the mol ratio of front Perovskite Phase lead titanates, and is uniformly mixed, obtains suspension；
3) by step 2) prepare suspension join in reactor inner bag, stirring lower addition mass concentration is the ammonia of 30%, ammonia volume is the 1/5 of the volumes of aqueous ethanol of tetra-n-butyl titanate, after being uniformly mixed, the reaction mass volume added in deionized water regulation reactor inner bag reaches the 70% of reactor inner bag volume, and is again stirring for mix homogeneously；
4) the reactor inner bag that step 3) is configured with reaction mass is placed in reactor, seal, after reacting 12 hours at 200 DEG C, reactor is allowed to naturally cool to room temperature, after unloading still, use absolute ethanol washing product, filter, dry, obtain the heterojunction composite of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide；
5) composite step 4) prepared is under air atmosphere, calcines 1 h, obtain the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide at 650 DEG C.
The preparation method of front Perovskite Phase lead titanate monocrystal nano line described in the present invention refers to Zhejiang University's thesis for the doctorate perovskite and preparation, structure and the performance of front perovskite oxide nano material, and author calls brightness together for appointing.
The present invention uses hydro-thermal reaction and the method for subsequent high temperature calcining, using the ethanol solution of tetra-n-butyl titanate and front Perovskite Phase lead titanate monocrystal nano line as the reaction mass of hydro-thermal reaction, anatase phase titanium dioxide is obtained by the hydrolysis of tetra-n-butyl titanate, using ammonia as mineralizer, and add deionized water to promote the hydrolysis of tetra-n-butyl titanate, it is then transferred in reactor, airtight hydrothermal treatment consists at 200 DEG C, obtains the hetero-junctions of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide.Subsequently the product obtained is carried out follow-up high-temperature process, it is achieved thereby that the preparation of the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide.
Present invention process, in implementation process, does not introduce other foreign ion, so having only to after hydro-thermal by washing with alcohol.Present invention process process is simple, it is easy to control, pollution-free, low cost, it is easy to produce.
Accompanying drawing explanation
Fig. 1 is the XRD figure spectrum of the Perovskite Phase lead titanate monocrystal nano line prepared of the present invention and the hetero-junctions of anatase phase titanium dioxide；
Fig. 2 is the SEM picture of the Perovskite Phase lead titanate monocrystal nano line prepared of the present invention and the hetero-junctions of anatase phase titanium dioxide；
Fig. 3 is the TEM collection of illustrative plates of the Perovskite Phase lead titanate monocrystal nano line prepared of the present invention and the hetero-junctions of anatase phase titanium dioxide；
Fig. 4 is the UV-Visible absorption figure of the Perovskite Phase lead titanate monocrystal nano line prepared of the present invention and hetero-junctions degradation of methylene blue (MB) different time of anatase phase titanium dioxide.
Detailed description of the invention
The present invention is further illustrated below in conjunction with embodiment.
Embodiment 1
1) tetra-n-butyl titanate is dissolved in 25ml ethanol, is made into Ti4+Concentration is the ethanol solution of 0.035mol/L, and stirs to being completely dissolved；
2) Perovskite Phase lead titanate monocrystal nano line before adding in the ethanol solution of the tetra-n-butyl titanate prepared to step 1) so that tetra-n-butyl titanate is 0.267:1 with the mol ratio of front Perovskite Phase lead titanates, and is uniformly mixed, and obtains suspension；
3) by step 2) prepare suspension join in reactor inner bag, stirring lower addition 5ml mass concentration is the ammonia of 30%, after being uniformly mixed, the reaction mass volume added in deionized water regulation reactor inner bag reaches the 70% of reactor inner bag volume, and is again stirring for mix homogeneously；
4) the reactor inner bag that step 3) is configured with reaction mass is placed in reactor, seal, after reacting 12 hours at 200 DEG C, reactor is allowed to naturally cool to room temperature, after unloading still, use absolute ethanol washing product, filter, dry, obtain the heterojunction composite of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide；
5)
Composite step 4) prepared, under air atmosphere, calcines 1 at 650 DEG C
H, obtains the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide.
Embodiment 2
1) tetra-n-butyl titanate is dissolved in 25ml ethanol, is made into Ti4+Concentration is the ethanol solution of 0.047mol/L, and stirs to being completely dissolved；
2) Perovskite Phase lead titanate monocrystal nano line before adding in the ethanol solution of the tetra-n-butyl titanate prepared to step 1) so that tetra-n-butyl titanate is 0.356:1 with the mol ratio of front Perovskite Phase lead titanates, and is uniformly mixed, and obtains suspension；
3) by step 2) prepare suspension join in reactor inner bag, stirring lower addition 5ml mass concentration is the ammonia of 30%, after being uniformly mixed, the reaction mass volume added in deionized water regulation reactor inner bag reaches the 70% of reactor inner bag volume, and is again stirring for mix homogeneously；
4) the reactor inner bag that step 3) is configured with reaction mass is placed in reactor, seal, after reacting 12 hours at 200 DEG C, reactor is allowed to naturally cool to room temperature, after unloading still, use absolute ethanol washing product, filter, dry, obtain the heterojunction composite of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide；
5)
Composite step 4) prepared, under air atmosphere, calcines 1 at 650 DEG C
H, obtains the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide.Its XRD figure spectrum is shown in Fig. 1, as seen from the figure gained peak be Perovskite Phase lead titanates with anatase phase titanium dioxide superpose peak, without other impurity peaks.Its SEM figure is shown in Fig. 2, TEM collection of illustrative plates is shown in that (deeper contrast region is lead titanates to Fig. 3, shallower contrast region is titanium dioxide), from Fig. 2 and Fig. 3, the Perovskite Phase lead titanate monocrystal nano line prepared can preferably be grown on Perovskite Phase lead titanate monocrystal nano line with the titanium dioxide in the hetero-junctions of anatase phase titanium dioxide, titania nanoparticles distribution ratio is more uniform, and does not occur than more serious reunion；(catalyst amount is the every 100 ml methylene blue solutions of 0.1g to its catalysis methylene blue, and the concentration of methylene blue solution is 10-5Mol/L) effect such as Fig. 4, As time goes on, the absorbance of solution is substantially reduced, it can be seen that the visible light catalytic efficiency of the composite of gained is higher.
Embodiment 3
1) tetra-n-butyl titanate is dissolved in 25ml ethanol, is made into Ti4+Concentration is the ethanol solution of 0.059mol/L, and stirs to being completely dissolved；
2) Perovskite Phase lead titanate monocrystal nano line before adding in the ethanol solution of the tetra-n-butyl titanate prepared to step 1) so that tetra-n-butyl titanate is 0.445:1 with the mol ratio of front Perovskite Phase lead titanates, and is uniformly mixed, and obtains suspension；
3) by step 2) prepare suspension join in reactor inner bag, stirring lower addition 5ml mass concentration is the ammonia of 30%, after being uniformly mixed, the reaction mass volume added in deionized water regulation reactor inner bag reaches the 70% of reactor inner bag volume, and is again stirring for mix homogeneously；
4) the reactor inner bag that step 3) is configured with reaction mass is placed in reactor, seal, after reacting 12 hours at 200 DEG C, reactor is allowed to naturally cool to room temperature, after unloading still, use absolute ethanol washing product, filter, dry, obtain the heterojunction composite of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide；
5)
Composite step 4) prepared, under air atmosphere, calcines 1 at 650 DEG C
H, obtains the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide.
Embodiment 4
1) tetra-n-butyl titanate is dissolved in 25ml ethanol, is made into Ti4+Concentration is the ethanol solution of 0.082mol/L, and stirs to being completely dissolved；
2) Perovskite Phase lead titanate monocrystal nano line before adding in the ethanol solution of the tetra-n-butyl titanate prepared to step 1) so that tetra-n-butyl titanate is 0.623:1 with the mol ratio of front Perovskite Phase lead titanates, and is uniformly mixed, and obtains suspension；
3) by step 2) prepare suspension join in reactor inner bag, stirring lower addition 5ml mass concentration is the ammonia of 30%, after being uniformly mixed, the reaction mass volume added in deionized water regulation reactor inner bag reaches the 70% of reactor inner bag volume, and is again stirring for mix homogeneously；
4) the reactor inner bag that step 3) is configured with reaction mass is placed in reactor, seal, after reacting 12 hours at 200 DEG C, reactor is allowed to naturally cool to room temperature, after unloading still, use absolute ethanol washing product, filter, dry, obtain the heterojunction composite of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide；
5) composite step 4) prepared is under air atmosphere, calcines 1 h, obtain the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide at 650 DEG C.
Claims (3)
1. the preparation method of the hetero-junctions of a Perovskite Phase lead titanate monocrystal nano line and anatase phase titanium dioxide, it is characterised in that comprise the following steps:
1) tetra-n-butyl titanate is dissolved in ethanol, regulate Ti4+Concentration is 0.035 ~ 0.082mol/L, and stirs to being completely dissolved;
2) Perovskite Phase lead titanate monocrystal nano line before adding in the ethanol solution of the tetra-n-butyl titanate prepared to step 1), regulation tetra-n-butyl titanate is 0.267 ~ 0.623:1 with the mol ratio of front Perovskite Phase lead titanates, and is uniformly mixed, obtains suspension；
3) by step 2) prepare suspension join in reactor inner bag, stirring lower addition mass concentration is the ammonia of 30%, ammonia volume is the 1/5 of the volumes of aqueous ethanol of tetra-n-butyl titanate, after being uniformly mixed, the reaction mass volume added in deionized water regulation reactor inner bag reaches the 70% of reactor inner bag volume, and is again stirring for mix homogeneously；
4) the reactor inner bag that step 3) is configured with reaction mass is placed in reactor, seal, after reacting 12 hours at 200 DEG C, reactor is allowed to naturally cool to room temperature, after unloading still, use absolute ethanol washing product, filter, dry, obtain the heterojunction composite of front Perovskite Phase lead titanate monocrystal nano line and titanium dioxide;
5) composite step 4) prepared is under air atmosphere, calcines 1 h, obtain the hetero-junctions of Perovskite Phase lead titanate monocrystal nano line and titanium dioxide at 650 DEG C.
Perovskite Phase lead titanate monocrystal nano line the most according to claim 1 and the preparation method of the hetero-junctions of anatase phase titanium dioxide, is characterized in that described reactor is polytetrafluoroethylliner liner, the reactor that rustless steel external member is airtight.
Perovskite Phase lead titanate monocrystal nano line the most according to claim 1 and the preparation method of the hetero-junctions of anatase phase titanium dioxide, is characterized in that the purity of described tetra-n-butyl titanate, ethanol and ammonia is all not less than analytical pure.
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| CN104772148A (en) * | 2015-04-03 | 2015-07-15 | 马鞍山锐凯特新材料有限公司 | Preparation method of perovskite type air purification photocatalyst |
| CN104831256A (en) * | 2015-04-03 | 2015-08-12 | 浙江大学 | Preparation method of lead titanate/titanium dioxide two dimensional monocrystalline heterojunction visible light catalyst |
| CN108031463A (en) * | 2017-11-13 | 2018-05-15 | 哈尔滨理工大学 | A kind of rutile/anatase titanium dioxide/titanium acid lithium lead and preparation method |
| CN114684786A (en) * | 2020-12-25 | 2022-07-01 | 江苏康润净化科技有限公司 | Method for efficiently producing hydrogen and oxygen based on perovskite titanium dioxide heterostructure |
| CN115121242B (en) * | 2022-06-08 | 2023-12-22 | 浙江理工大学 | Perovskite phase hierarchical structure lead titanate-titanium dioxide composite photocatalyst, preparation method and application |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101318696A (en) * | 2008-07-23 | 2008-12-10 | 黑龙江大学 | Method for concocting and synthesizing nano-titanium dioxide with high-temperature stability by using aqueous ammonia |
| CN101618889A (en) * | 2009-08-03 | 2010-01-06 | 浙江大学 | Method for preparing lead titanate nano column automatically assembled by perovskite structure nano pieces |
| CN102517637A (en) * | 2011-12-29 | 2012-06-27 | 洛阳理工学院 | Preparation method for lead titanate nanowire |
| CN102995120A (en) * | 2012-12-12 | 2013-03-27 | 国家纳米科学中心 | Nanometer TiO2 monocrystalline material, preparation method and application thereof |
| CN103603030A (en) * | 2013-10-22 | 2014-02-26 | 浙江大学 | Preparation method of lead titanate monocrystal nano fiber with controllable size and one-dimensional columnar structure |
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Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101318696A (en) * | 2008-07-23 | 2008-12-10 | 黑龙江大学 | Method for concocting and synthesizing nano-titanium dioxide with high-temperature stability by using aqueous ammonia |
| CN101618889A (en) * | 2009-08-03 | 2010-01-06 | 浙江大学 | Method for preparing lead titanate nano column automatically assembled by perovskite structure nano pieces |
| CN102517637A (en) * | 2011-12-29 | 2012-06-27 | 洛阳理工学院 | Preparation method for lead titanate nanowire |
| CN102995120A (en) * | 2012-12-12 | 2013-03-27 | 国家纳米科学中心 | Nanometer TiO2 monocrystalline material, preparation method and application thereof |
| CN103603030A (en) * | 2013-10-22 | 2014-02-26 | 浙江大学 | Preparation method of lead titanate monocrystal nano fiber with controllable size and one-dimensional columnar structure |
Non-Patent Citations (1)
| Title |
|---|
| 单晶钛酸铅纳米结构的可控制备、掺杂、相变与应用研究;肖珍;《中国优秀博士论文全文数据库 工程科技I辑》;20130815;摘要，第110页倒数第2段至第111页第1段，第134页倒数第2段，第148页小结 * |
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